# Colonna Brothers Inc., North Bergen, NJ – FDA Inspections

Source: https://www.keypedia.com/companies/colonna-brothers-inc/61ee0ad0-c30a-4291-ac24-f2b846fa11db

> Inspection records and compliance data for Colonna Brothers Inc. in North Bergen, New Jersey. 11 FDA inspections on record, last inspected April 28, 2025.

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## Details

- Name: Colonna Brothers Inc.
- FEI Number: 2215071
- Address Line 1: 4102 Bergen Tpke
- City: North Bergen
- State: New Jersey
- Zip Code: 07047
- Country Name: United States
- Address: 4102 Bergen Tpke, North Bergen, New Jersey 07047, United States
- Country: United States

## Related Documents

- FDA Inspection 1268983 - Colonna Brothers Inc. - 2025-04-28 — source: FDA, date: April 28, 2025
- FDA Inspection 1178787 - Colonna Brothers Inc. - 2022-08-16 — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2022
- FDA Inspection 1107578 - Colonna Brothers Inc. - 2019-10-21 — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2019
- FDA Inspection 1080577 - Colonna Brothers Inc. - 2018-10-30 — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2018
- FDA Inspection 1037945 - Colonna Brothers Inc. - 2017-11-06 — classification: No Action Indicated (NAI), source: FDA, date: November 6, 2017
- FDA Inspection 996136 - Colonna Brothers Inc. - 2016-12-20 — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2016
- FDA Inspection 968457 - Colonna Brothers Inc. - 2016-03-30 — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2016
- [FDA Inspection 968457 - Colonna Brothers Inc. - 2016-03-30](https://www.keypedia.com/records/fda_inspections/colonna-brothers-inc/c34a7b74-8469-4845-b6ff-0e8b598f5093) — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2016
- FDA Inspection 886241 - Colonna Brothers Inc. - 2014-06-30 — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2014
- FDA Inspection 886241 - Colonna Brothers Inc. - 2014-06-30 — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2014

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